Canonical Allele Identifier: CA1548129243
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859859C= , CM000667.2:g.56859859C= GRCh38
NC_000005.9:g.56155686C= , CM000667.1:g.56155686C= GRCh37
NC_000005.8:g.56191443C= NCBI36
NG_031884.1:g.49787C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.778C= MANE Select ENSP00000382423.3:p.Arg260=
ENST00000399503.3:c.778C= ENSP00000382423.3:p.Arg260=
NM_005921.1:c.778C= NP_005912.1:p.Arg260=
XM_005248519.3:c.400C= XP_005248576.2:p.Arg134=
XM_011543406.1:c.523C= XP_011541708.1:p.Arg175=
XM_011543407.1:c.778C= XP_011541709.1:p.Arg260=
XM_011543408.1:c.778C= XP_011541710.1:p.Arg260=
XM_017009484.1:c.367C= XP_016864973.1:p.Arg123=
XM_017009485.1:c.289C= XP_016864974.1:p.Arg97=
XR_001742068.2:n.809C=
NM_005921.2:c.778C= MANE Select NP_005912.1:p.Arg260=